TY - JOUR
T1 - Polycyclic guanidine natural products
T2 - Total synthesis of batzelladines
AU - Ueda, Hirofumi
N1 - Publisher Copyright:
© Society of Synthetic Organic Chemistry. All rights reserved.
PY - 2019
Y1 - 2019
N2 - In nature, there are a number of natural products containing guanidine moiety. Among them, polycyclic guanidine compounds have attracted considerable attention from synthetic chemists and biologists because of their architecturally intriguing structures and potent biological activities. This short review summarizes synthetic methodologies toward batzelladines focusing on stereoselective construction of the core tricyclic guanidine skeleton.
AB - In nature, there are a number of natural products containing guanidine moiety. Among them, polycyclic guanidine compounds have attracted considerable attention from synthetic chemists and biologists because of their architecturally intriguing structures and potent biological activities. This short review summarizes synthetic methodologies toward batzelladines focusing on stereoselective construction of the core tricyclic guanidine skeleton.
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U2 - 10.5059/yukigoseikyokaishi.77.71
DO - 10.5059/yukigoseikyokaishi.77.71
M3 - Article
AN - SCOPUS:85060892998
SN - 0037-9980
SP - 71
EP - 74
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
ER -